A total of 303 infants with esophageal atresia and/or tracheoesophagea
l fistula were treated over 10 years (1980-1989). The overall survival
rate was 86.5%. Associated anomalies were identified in 51.8% of pati
ents, the most common being cardiac malformations which affected 24.4%
of infants and was responsible for the majority of deaths. The dramat
ic increase in survival of infants with esophageal atresia in the past
half century is due to improvements in pre- and postoperative managem
ent, meticulous operative technique to reduce anastomotic complication
s, and aggressive treatment of associated congenital anomalies.